|Publication number||US7226541 B2|
|Application number||US 10/738,628|
|Publication date||Jun 5, 2007|
|Filing date||Dec 16, 2003|
|Priority date||Jun 20, 2001|
|Also published as||US20040191894, WO2002102500A1|
|Publication number||10738628, 738628, US 7226541 B2, US 7226541B2, US-B2-7226541, US7226541 B2, US7226541B2|
|Inventors||Heinz-Joachim Muller, Daniel Mullette|
|Original Assignee||Siemens Water Technology Corp.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (122), Non-Patent Citations (14), Referenced by (48), Classifications (33), Legal Events (12)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation, under 35 U.S.C. § 120, of International patent application Ser. No. PCT/AU02/00784, filed on Jun. 14, 2002 under the Patent Cooperation Treaty (PCT), which was published by the International Bureau in English on Dec. 27, 2002, which designates the U.S. and claims the benefit of Australian Provisional Patent Application No. PR 5843, filed Jun. 20, 2001.
The invention relates to compositions suitable for use in forming membranes, in particular for forming hollow fiber membranes for use in microfiltration. The invention also relates to membranes prepared from such compositions, and to methods of their preparation.
The following discussion is not to be construed as an admission with regard to the common general knowledge in Australia.
Synthetic membranes are used for a variety of applications including desalination, gas separation, filtration, and dialysis. The properties of the membranes vary depending on the morphology of the membrane i.e. properties such as symmetry, pore shape and pore size and the polymeric material used to form the membrane.
Different membranes can be used for specific separation processes, including microfiltration, ultrafiltration, and reverse osmosis. Microfiltration and ultrafiltration are pressure driven processes and are distinguished by the size of the particle or molecule that the membrane is capable of retaining or passing. Microfiltration can remove very fine colloidal particles in the micrometer and submicrometer range. As a general rule, microfiltration can filter particles down to 0.1 μm, whereas ultrafiltration can retain particles as small as 0.01 μm and smaller. Reverse Osmosis operates on an even smaller scale.
As the size of the particles to be separated decreases, the pore size of the membrane decreases and the pressure required to carry out the separation increases.
A large surface area is needed when a large filtrate flow is required. One known technique to make filtration apparatus more compact is to form a membrane in the shape of a hollow porous fiber. Modules of such fibers can be made with an extremely large surface area per unit volume.
Microporous synthetic membranes are particularly suitable for use in hollow fibers and are produced by phase inversion. In this process, at least one polymer is dissolved in an appropriate solvent and a suitable viscosity of the solution is achieved. The polymer solution can be cast as a film or hollow fiber, and then immersed in precipitation bath such as water. This causes separation of the homogeneous polymer solution into a solid polymer and liquid solvent phase. The precipitated polymer forms a porous structure containing a network of uniform pores. Production parameters that affect the membrane structure and properties include the polymer concentration, the precipitation media and temperature and the amount of solvent and non-solvent in the polymer solution. These factors can be varied to produce microporous membranes with a large range of pore sizes (from less than 0.1 to 20 μm), and altering chemical, thermal and mechanical properties.
Microporous phase inversion membranes are particularly well suited to the application of removal of viruses and bacteria. Of all types of membranes, the hollow fiber contains the largest membrane area per unit volume.
Flat sheet membranes are prepared by bringing a polymer solution consisting of at least one polymer and solvent into contact with a coagulation bath. The solvent diffuses outwards into the coagulation bath and the precipitating solution will diffuse into the cast film. After a given period of time, the exchange of the non-solvent and solvent has proceeded such that the solution becomes thermodynamically unstable and demixing occurs. Finally, a flat sheet is obtained with an asymmetric or symmetric structure.
Hydrophobic surfaces are defined as “water hating” and hydrophilic surfaces as “water loving”. Many of the polymers that porous membranes are made of are hydrophobic polymers. Water can be forced through a hydrophobic membrane by use of sufficient pressure, but the pressure needed is very high (150–300 psi), and a membrane may be damaged at such pressures and generally does not become wetted evenly.
Hydrophobic microporous membranes are characterized by their excellent chemical resistance, biocompatibility, low swelling and good separation performance. Thus, when used in water filtration applications, hydrophobic membranes need to be hydrophilized or “wet out” to allow water permeation. Some hydrophilic materials are not suitable for microfiltration and ultrafiltration membranes that require mechanical strength and thermal stability since water molecules can play the role of plasticizers.
Currently, poly(tetrafluoroethylene) (PTFE), Polyethylene (PE), Polypropylene (PP) and poly(vinylidene fluoride) (PVDF) are the most popular and available hydrophobic membrane materials. Poly(vinylidene fluoride) (PVDF) is a semi-crystalline polymer containing a crystalline phase and an amorphous phase. The crystalline phase provides good thermal stability whilst the amorphous phase adds some flexibility to the membrane. PVDF exhibits a number of desirable characteristics for membrane applications, including thermal resistance, reasonable chemical resistance (to a range of corrosive chemicals, including sodium hypochlorite), and weather (UV) resistance.
While PVDF has to date proven to be the most desirable material from a range of materials suitable for microporous membranes, the search continues for membrane materials which will provide better chemical stability and performance while retaining the desired physical properties required to allow the membranes to be formed and worked in an appropriate manner.
In particular, a membrane is required which has a superior resistance (compared to PVDF) to more aggressive chemical species, in particular, oxidizing agents such as sodium hypochlorite and to conditions of high pH i.e. resistance to caustic solutions.
According to a first aspect the invention provides the use of polymer suitable for forming into an ultrafiltration or microfiltration membrane, said polymer being a terpolymer of tetrafluoroethylene (TFE), PVDF and hexafluoropropylene monomers.
Preferably, the polymer includes from 20–65% PVDF monomer, from 10–20% hexafluoropropylene monomer and 30–70% TFE.
More preferably, the polymer includes from 30–50% PVDF monomer, from 15–20% hexafluoropropylene, and from 30–55% TFE. Even more preferably, the polymer includes from 35–40% PVDF and 17–20% HFP and 40–48% TFE.
Most preferably, the polymer is a terpolymer of 44.6% tetrafluoroethylene (TFE) monomers, 36.5% PVDF monomers, and 18.9% hexafluoropropylene monomers.
Unless otherwise indicated, all percentages are expressed as weight percentages.
According to a second aspect the invention provides an ultrafiltration and/or microfiltration membrane formed from a terpolymer including TFE monomers, PVDF monomer and hexafluoropropylene monomer. Preferably the monomer composition is approximately 44.6% tetrafluoroethylene (TFE) monomer, 36.5% PVDF monomer and 18.9% hexafluoropropylene monomer.
The membranes of the second aspect have an improved chemical stability to oxidizing agents and caustic soda relative to a membrane formed from PVDF alone.
According to a third aspect the invention provides a method of manufacturing a microfiltration or ultrafiltration membrane including the step of casting a membrane from a composition including a terpolymer of 44.6% tetrafluoroethylene (TFE) monomer, 36.5% PVDF monomer and 18.9% hexafluoropropylene monomer.
Preferably, the membrane is in the form of a hollow fiber, cast by the TIPS procedure, or more preferably by the DIPS procedure.
Most preferably, the polymer used is THV 220G, obtained from DyneonŽ (3M) as a solvent soluble fluoropolymer. The polymer is a combination of approximately 44.6% tetrafluoroethylene (TFE) monomer, 36.5% PVDF monomer, and 18.9% hexafluoropropylene monomer.
According to a fourth aspect, the invention provides a method of forming a polymeric ultrafiltration or microfiltration membrane including the steps of:
preparing a leachant resistant membrane dope;
incorporating a leachable pore forming agent into the dope;
casting a membrane; and
leaching said leachable pore forming agent from said membrane with said leachant.
Preferably, the leachant resistant membrane polymer includes a terpolymer of TFE, PVDF, and hexafluoropropylene. More preferably, the polymer includes 44.6% tetrafluoroethylene (TFE) monomers, 36.5% PVDF monomers, and 18.9% hexafluoropropylene monomers.
Preferably, the leachable pore forming agent is silica, and the leachant is a caustic solution, but the pore forming agent may for preference be any inorganic solid with an average particle size less than 1 micron while the leachant may be any material/solution that leaches the said pore forming agent from the membrane.
According to fifth aspect, the invention provides a method of improving the structure of a polymeric ultrafiltration or microfiltration membrane by the addition of a nucleating agent to a membrane dope. Preferably the nucleating agent is added in catalytic amounts and most preferably it is TiO2, however, any insoluble/inert (unleachable) inorganic solid with an average particle size less than 1 micron may be used.
According to a sixth aspect, the invention provides an elastic polymeric ultrafiltration or microfiltration membrane having an asymmetric cross section defining a large-pore face and a small-pore face; said membrane having a higher flux at a given pressure from said large-pore face to said small-pore face than from said small-pore face to said large-pore face.
Preferably the elastic membrane is formed from the preferred membrane forming mixtures of the preceding aspects, and may also be formed using the addition of leachable pore forming agents and/or nucleating agents.
The invention will now be described with particular reference to specific examples. It will be appreciated, however, that the inventive concept disclosed therein is not limited to these specific examples
THV 220G, obtained from DyneonŽ Corp (3M) was dissolved in N-methylpyrrolidone (NMP) at approximately 20 wt. %. A flat sheet membrane was cast from this solution and precipitated in water at 60° C. before being examined using scanning electron microscopy (SEM).
A standard DIPS process was employed as follows: Polymer solutions were mixed and heated to around 50° C. and pumped (spun) through a die into a 5 meter water-filled quench (or solidification) bath at 65° C. Non-solvent (lumen) consisting of 20% NMP, 10% water and 70% polyethylene glycol (PEG200) was fed through the inside of the die to form the lumen. The hollow fiber was then spun into the quench bath and solidified, before being run out of the bath over driven rollers onto a winder situated in a secondary water bath at room temperature to complete the quench and washing of the fiber.
The membrane structure was reasonable although a skin was found on the surface of the membrane that prevented exposure of surface pores.
The caustic resistance of the membrane was tested by placing a sample of the flat sheet into 5 wt. % caustic solution and comparing the appearance with a control of PVDF membrane cast by the TIPS process.
Both samples were thoroughly wet out with alcohol prior to immersion in the caustic solution. The THV samples become transparent upon complete wetting. The results of the caustic immersion test are shown in table 1.
Table 1 shows the results of the caustic resistance tests. The results indicate that while the membranes are not impervious to caustic, as would be the case for a material like Teflon, they show extremely limited degradation for an extended period of time in a comparatively strong caustic solution. All subsequent exposures to 5% solutions have shown the same result, that a slight yellowing occurs upon immediate contact with the solution but no further degradation (either visually or affecting the membrane properties) occurs.
In addition to color changes, the stiffness of both the PVDF and the THV samples were examined. The PVDF membrane had lost a marked amount of flexibility and was quite brittle, while by contrast, the THV sample appeared to be relatively unaffected.
The results strongly suggest that no detrimental modification of the polymer membranes takes place as a result of such caustic immersion.
TABLE 1 Date/Time elapsed THV 200 Sheet PVDF Fiber (TIPS) 5 mins Colorless Light brown 10 mins Colorless Light brown 1 hr Colorless Darker brown 2 days 19 hrs Colorless Dark brown/reddish 3 days Very slight yellowing Very dark brown 3 days 18 hrs Very slight yellowing Very dark brown 4 days Very slight yellowing Very dark brown 5 days Very slight yellowing Slightly darker/coppery 6 days Very slight yellowing Slightly darker/coppery 7 days Very slight yellowing Very dark turning black 10 days Very slight yellowing Very dark turning black 11 days Very slight yellowing Very dark turning black
Modification of Membrane Hydrophobicity/Hydrophilicity
Those skilled in the art will appreciate the desirability of preparing membranes that are hydrophilic in character. For instance, as described earlier hydrophilic membranes are simpler to operate than hydrophobic membranes as they do not require an additional wetting step.
It was established in the present case that THV 220G is compatible with Lutonal A25 (Polyvinylethylether) at concentrations of around 2%. Lutonal A25 makes the DIPS membranes of the present application less hydrophobic.
Other than modifying hydrophobicity, the addition of Lutonal A25 appeared to make little difference in the physical structure of the membrane, apart from opening the membrane structure slightly. However membranes prepared with or without Lutonal are still acceptable in terms of their structure.
The addition of Lutonal A25 reduced the mixing time of the dopes quite dramatically.
Other elements of the DIPS process have also been investigated in conjunction with the use of THV 220G as a membrane polymer. It was found that non solvents can be used in a dope mix such as the addition of 5% glycerine triacetate (GTA) into the mixture without undue detrimental effects.
In order to produce membranes without a dense surface skin and having a more hydrophilic nature, silica was added to the dope with the intention of leaching the silica out of the matrix by the use of a caustic solution.
A hydrophilic silica Aerosil 200 and a hydrophobic silica Aerosil R972 were tested separately as additives to the THV 220G membrane mixture. The dopes were cast into flat sheet membranes, and were quenched in hot water at 60° C. as described previously. Once the membranes had been cast, a portion thereof was leached in a 5% aqueous caustic solution at room temperature for 14 hours. Without wishing to be bound by theory, it is believed that the silica reacts with caustic to make the membrane hydrophilic as discussed below. Also, the leaching using caustic soda provides a membrane of good open structure. A number of membranes containing silica were cast. The results are shown in Table 2.
18% THV, 8% Aerosil R972,
Very high viscosity
2% Lutonal A25, 72% NMP
21% THV, 5% Aerosil 200,
2% Lutonal A25, 72% NMP
20% THV, 10% R972,
Extremely viscous (paste-
2% Lutonal A25, 68% NMP
20% THV, 5% R972,
20% THV, 0.5% R972,
2% Lutonal A25, 77.5%
20% THV, 80% NMP
18% THV, 5% R972,
2% Lutonal A25, 75% NMP
20% THV, 5% R972,
Extreme viscosity - Far
5% Mg(OH)2, 2% Lutonal
too high to cast
A25, 68% NMP
Table 2 demonstrates that the silica is required in reasonably high concentrations to make the membranes hydrophilic. It also shows the trend of increasing viscosity with increasing silica content.
After the membranes were cast, and prior to leaching, the membranes were examined using scanning electron microscopy. The structures were generally extremely promising with the surface of the sheets completely open and totally free of any skin. The cross-sectional appearance was more like a conglomerate of precipitated particles, rather than a true honeycomb like structure.
The best form of the silica appeared to be the hydrophobic Aerosil R972, although both forms of silica produced a hydrophilic membrane with a highly porous structure.
Subsequently placing the sample in caustic soda to leach the silica provided a dramatic opening up in the membrane structure even further. The result of the leaching was a change in the cross-section from the abovementioned conglomerate-like structure to the more traditional lace or sponge-like formation.
The optimal dope for forming a DIPS polymer appears to be from a mixture of 72% NMP, 20% THV, 6% silica and 2% Lutonal. This provides a hydrophilic membrane from a dope possessing a viscosity in the range that can be easily pumped.
A number of hollow fiber membranes were prepared from the above dope. The wetting characteristics were as desired and the membrane structure showed an extremely open surface. While 6% silica Was used in the present invention, it will be appreciated that the quantity can vary significantly without departing from the present inventive concept.
Fibers incorporating silica with thicker walls were prepared and the current properties of the fiber membranes were examined. The fiber was then subject to leaching with a 5% caustic solution at room temperature for 18 hours.
It can be seen that leaching the membrane changes the permeability and bubble points significantly without altering the desirable physical properties of the membrane. The leaching of the silica from the membranes has a positive effect upon permeability.
Thus, before leaching, the membrane had very few pores and extremely low flows. After leaching, however, the situation is reversed and there are a multitude of pores and a high flux.
A long leaching time is not necessarily required and can be incorporated in the production process as a post-treatment of the final modular product. The leaching process can be carried out at any time, however there is an advantage to postponing the leaching process as long as possible, since any damage to the surface of the fibers during handling can be overcome by leaching which physically increases the porosity of the membrane. Existing PVDF membrane surfaces can be damaged irreconcilably during production, resulting in a decrease in permeability and flux of the fibers.
SEM analysis of the membranes showed a high degree of asymmetry. Asymmetry is defined as a gradual increase in pore size throughout the membrane cross-section, such that the pores at one surface of the hollow fiber are larger than the other. In this case, the pore size increase was seen from the outer surface where the pores were smallest (and a quite dense surface layer was present) to the inner surface where the pores were significantly larger than those on the outer surface.
Preparation of the fibers was run at 65° C. rather than 50° C. as in a typical DIPS process. Increasing the quench bath temperature by 10–15° C. dramatically affects the surface structure. The higher temperature gives a much more open surface. The use of the higher temperatures therefore accordingly means it is feasible to increase the polymer concentrations and possibly the silica concentration if it is desired to bolster the existing membrane and increase the mechanical strength.
Further it has been found that a more particular mixing procedure contributes to the success of forming a membrane of high permeability. Mixing constituents together in a random manner does not produce such a good result as following a more stringent procedure whereby the Aerosil R972 is dissolved in the total quantity of NMP and this solution is allowed to degas. The polymer pellets are mixed with the liquid Lutonal A25 to coat the pellets. When these two procedures are complete, the two mixtures are combined. The advantage of this appears to be that the silica is dispersed effectively and does not clump (which can lead to macrovoids) and also, the pellets do not clump (which has the effect of increasing mixing time and consistency of the dope) since they are coated with a sufficient quantity of Lutonal A25 for a sufficient time to allow them to dissolve individually.
As well as silica, the leaching process allows for the introduction of other functionalities into the membrane, such as introducing hydrolyzable esters to produce groups for anchoring functional species to membranes.
Surprisingly, it has also been found that the membrane remains hydrophilic after leaching. Again, without wishing to be bound by theory, the silica particles have a size in the order of manometers so consequently the silica disperses homogeneously throughout the polymer solution. When the polymer is precipitated in the spinning process, there is a degree of encapsulation of the SiO2 particles within the polymer matrix. Some of the particles (or the conglomerates formed by several silica particles) are wholly encapsulated by the precipitating polymer, some are completely free of any adhesion to the polymer (i.e. they lie in the pores of the polymer matrix) and some of the particles are partially encapsulated by the polymer so that a proportion of the particle is exposed to the ‘pore’ or to fluid transfer.
When contacted with caustic, it is believed that these particles will be destroyed from the accessible side, leaving that part of the particle in touch with the polymer matrix remaining. The remainder of the silica particle adheres to the polymer matrix by hydrophobic interaction and/or mechanical anchoring. The inside of the particle wall is hydrophilic because it consists of OH groups attached to silica. Because the silica is connected to hydrophobic groups on the other side, it cannot be further dissolved.
Thus, when the membranes are treated with caustic solution, the free unencapsulated SiO2 reacts to form soluble sodium silicates, while the semi-exposed particles undergo a partial reaction to form a water-loving surface (bearing in mind that given the opportunity, such particles would have dissolved fully). It is believed that the pores in the polymer matrix formed during the phase inversion stage yet filled with SiO2 particles are cleaned out during leaching, giving a very open, hydrophilic membrane.
TiO2 (titania) was also added to the membrane at a variety of concentrations. TiO2 has been added to membrane forming mixtures previously as a filler to provide abrasion resistance or to act as a nucleating agent, to increase the rate of fiber solidification.
However, surprisingly in the present case, it was found that the addition of TiO2 in concentrations below that used for reinforcement of membranes, a high degree of asymmetry was introduced into the membranes. In particular, this was as a result of the formation of a dense outer layer. Without wishing to be bound by theory, the applicant believes that the TiO2 particles provide a site for phase inversion or precipitation to begin. In hollow fiber membranes prepared by the DIPS process, the high number of fast solidification sites at which precipitation occurs means that the pores formed near the membrane surface are smaller, fewer and further between.
The use of too much titania can cause a dense outer layer on the membrane to restrict permeability. Further, as the titania disperses very well throughout the dope, only of the order of a catalytic amount is required. For example, only about 0.1–0.2 wt. % titania need be incorporated into the membrane, although as much as 3% can be used depending on the desired effect.
A dope formulation giving good results is 20 wt. % THV 220G, 6 wt. % Aerosil R972, 2 wt. % Lutonal A25, 0.2 wt. % TiO2, and 71.8 wt. % N-methylpyrrolidone.
A dope having the above formulation was mixed and cast according to the DIPS method. They were then leached in 5% caustic soda solution for approximately 24 hours and then soaked in glycerol. Soaking fibers in glycerol or the like is a highly desirable step, since the material is relatively flexible and will allow pores to collapse. The results for the TiO2 trial fibers are given as Table 3.
Results for THV 200
Bubble Point (kPa)
Burst Point (kPa)
Break Extension (%)
Fiber Dimensions (μM)
1080 OD, 535 ID
Break Force per unit area (N/cm2)
Table 3 lists the properties of the membranes made which incorporate a small proportion of TiO2. The most apparent property to note is the high permeability of the membrane.
High Polymer Concentrations
Attempts at making polymer concentrations above 20 wt. % were attempted. Doing so however caused alternative problems mainly based around a dramatic increase in viscosity. Once the polymer portion rises to above 25 wt. %, viscosity becomes too high to pump in conventional pumps. However, high polymer concentrations were seen to correlate with an increase in the mechanical strength of the membrane. Optimal results of workability and strength were achieved with the hollow fiber having a polymer concentration of 22%. The best was seen to be 22 wt. % THV 220G, 6 wt. % Aerosil R972, 2 wt. % Lutonal A25 and 70 wt. % N-methylpyrrolidone. Concentrations as high as 30 wt. % polymer did produce a feasible membrane. The high polymer concentration membranes were leached in a 5% caustic solution for 24 hours and then soaked in glycerol. The results are shown in Table 4. A point of note is that the increase in polymer concentration or the addition of TiO2 does not appear to improve the bubble point or burst pressure of the fibers in any way. The mechanical strength of the fiber appears to be mainly a function of wall thickness and lumen diameter.
Results for THV 200
Bubble Point (kPa)
Burst Point (kPa)
Break Extension (%)
Break Force (N)
Fiber Dimensions (μM)
930 OD, 542 ID
Break Force per unit area (N/cm2)
Table 4 lists the properties of the membrane made using 22% polymer (without TiO2). Comparing the results to Table 3, the membrane exhibit very similar characteristics with the exception that Table 3 indicates possibly a higher permeability/flux for titania containing membranes.
Physical Properties of Membranes
The bubble point measurements in Tables 3 and 4 do not give an entirely accurate determination of the bubble point, the pore size or molecular weight cut off of the membrane because the membranes are somewhat rubbery and flexible so that under pressure the membrane expands and hence the pores stretch like a rubber band. It has been observed that the fibers increase in size slightly under a backwash pressure of as low as 100 Kilopascals.
This behavior is apparently due to the high elastic nature of the polymer which also gives extremely high break tension described in Table 4. This elastic behavior would adequately describe the apparently low bubble point recorded for the membrane, since as the membrane is stretched by the pressure applied, the pores would be stretching proportional to the overall size increase of the fiber. This property is extremely valuable for cleaning a membrane, since the pores may be opened up by the application of a liquid backwash and any material fouling the pores may be easily dislodged and flushed away. The elastic behavior also indicates that the membrane (and hence the pores) may recover up to 100% of such a deformation, thus the pores would return to their original size.
To demonstrate this characteristic behavior, the permeability and fluxes of the fibers were measured. Permeability and flux are typically measured with a filtration direction (direction of the filtrate flow relative to the membrane surfaces) outside-in with the filtrate collected from the inside of the hollow fiber. To prove that the pore structure is increasing in size, the flow was reversed so that the filtration direction was inside-out, with filtrate emerging on the outer side of the fiber.
Table 5 shows the results of these “outside-in” and “inside-out” tests
Flux Outside-In (L/m2 ˇ hr)
Flux Inside-Out (L/m2 ˇ hr)
Table 5 and FIG. 1 show that the flux for inside-out flow increases as the pressure increases, while the outside-in flow remains almost completely constant. This indicates that the pressure applied from the inside is expanding the pores to allow far higher flows. This elasticity described is one of the most desirable properties of the membranes discussed.
As a result of this one of the desirable features of the membranes according to the present invention is their ability to be potted directly into epoxy. PVDF membranes require a more flexible potting material such as polyurethane to prevent damage to the fibers. PVDF fibers can break with relative ease if the fibers are potted in a potting material which lacks any flexibility. If there is no flexibility in the potting material there can be breakage of the fiber at the point where the fiber enters the pot. By contrast, the membranes of the invention can be potted into epoxy potting material and the fibers will not be significantly damaged during use. In fact, the membranes of the present invention can be stretched to the normal break extension of the fiber when pulled parallel to the pot surface i.e. 90° to the potted direction.
The comparison of the properties of the THV membranes of the present application and PVDF prepared with the DIPS process are shown in Table 6.
Break Extension (%)
Break Force (N)
Permeability (LMH @ 100 kPa)
Bubble Point (kPa)
Table 6 gives a comparison between THV membranes manufactured using the DIPS process and the best (to date) PVDF membranes manufactured using the DIPS process. The main differences are the spontaneous wetting of the THV membrane and also the high clean water permeability, both of which are lacking in current PVDF membranes. The other difference lies in comparing the stiffness of the membranes, which is directly attributable to the polymers used to produce the membrane.
It would be appreciated by those skilled in the art that while the invention has been described with particular reference to one embodiment, many variations are possible without deviating from the inventive concept disclosed herein.
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|U.S. Classification||210/500.36, 264/209.1, 210/500.42, 264/41, 264/211.16, 210/500.23, 210/500.27|
|International Classification||B01D71/36, B01D69/02, B01D71/32, B01D71/34, B29C47/88, B01D65/00, B01D69/08, B29C47/92, B01D67/00, B01D29/00|
|Cooperative Classification||B01D2323/22, B01D2325/30, B01D2325/022, B01D2323/02, B01D71/34, B01D69/02, B01D67/0018, B01D71/32, B01D69/08, B01D71/36|
|European Classification||B01D67/00K14H, B01D71/34, B01D69/08, B01D69/02, B01D71/36, B01D71/32|
|Jun 2, 2004||AS||Assignment|
Owner name: U. S. FILTER WASTEWATER GROUP, INC., PENNSYLVANIA
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